Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion description "[The combined results based on all studies showed that there was a statistically significant link between CCND1 G870A polymorphism and DTC risk (GG vs. AA: OR=0.83, 95%CI=0.71-0.96).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion evidence source_evidence_literature NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion SIO_000772 21606015 NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion wasDerivedFrom befree-20140225 NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_assertion wasGeneratedBy ECO_0000203 NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185716.RAtaWpotKw1kscoVWubt_SiLM5vFT30SgsGzyJE6hZ828130_provenance.